BEUDAMED
    FDA Adverse Event Injury Summary report: N

    GLATOPAJECT

    MDR report key: 25095236 · Received May 6, 2026

    Report

    Report Number
    MW5187774
    Event Type
    Injury
    Date Received
    May 6, 2026
    Date of Event
    October 7, 2025
    Report Date
    April 30, 2026
    Manufacturer
    SANDOZ, INC.
    Product Code
    KZH
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    SD, US
    Reporter Occupation
    PATIENT
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    I USE A GLATOPAJECT DEVISE FOR MY MULTIPLE SCLEROSIS MEDICATION. SEVERAL TIMES OVER THE LAST SEVERAL YEARS SINCE I WAS MOVED TO THE GENERIC MEDICATION, THIS GENERIC AUTO JET DEVICE STICKS/JAMS, CAUSE LOSS OF MEDICINE, BRUSHING, PAIN, ETC. I HAD A SEVERE REACTION TODAY, BUT A WORSE ONE BACK IN OCTOBER WHEN I HAD SEVERE BRUISING AND PAIN. HAD TO GO TO THE DOCTOR. I HAD A DEEP BRUISE, THAT TURNED HARD, AND IN TIME CAME TO THE SURFACE AND I HAD SKIN STABBING OVER. MY HUSBAND SAID I LOOKED LIKE A ZOMBIE. I NEVER HAD THESE ISSUES WITH THE COPAXONE DEVICE. THIS ONE FEELS CHEAP AND WORKS CHEAPLY AND CAUSES REGULAR ISSUES, AND MAKES ME WANT TO FORGO USING IT. ITS TRULY EXHAUSTING. I HATE THAT INSURANCE FORCED THIS MEDICINE CHANGE, AND NOW IM STUCK WITH A TERRIBLE DEVICE. THESE ISSUES WITH THE DEVICE HAPPEN VERY FREQUENTLY. TRULY, ITS A GARBAGE INJECTOR. FOR THE COST OF THE MEDICATION, YOU'D HOPE YOU'D FEEL CONFIDENT IN GETTING IT INJECTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    494516 GLATOPAJECT INTRODUCER, SYRINGE NEEDLE KZH SANDOZ, INC.

    Patients

    Seq Age Sex Outcome Treatment
    1 40 YR Female Required Intervention GLATIRAMER ACETATE | GLATOPAJECT | HYDROCHLOROTHIAZIDE| ZOLOFT HYDROCHLOROTHIAZIDE